Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Hemoglobin Lepore"'
Akademický článek
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Autor:
MR Ahmadi Fard, H Akhavan Niaki, H Mahmoodi Nesheli, A Banihashemi, M Azizi, N Mousavi, R Pourbagher, R Yousefi Kamangari
Publikováno v:
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 14, Iss 3, Pp 13-18 (2012)
BACKGROUND AND OBJECTIVE: Hereditary persistence of fetal hemoglobin (HPFH) and δβ-thalassemia are heterogeneous disorders characterized by elevated levels of fetal hemoglobin (Hb F). Deletional mutations are responsible for the disease and are not
Externí odkaz:
https://doaj.org/article/81fc2834a09f4abdb83e659b12c69211
Autor:
Harapin, Kristina
Hemoglobin je krvni pigment koji sadrži željezo. Nalazimo ga u crvenim krvnim stanicama, eritrocitima. Sastoji se od globinske skupine i hem skupine. Njegova uloga je prijenos kisika, iz pluća do stanica, i odnošenje ugljikovog dioksida, od stani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::27a6bd4f9ef079c1a05a069db94b3d3d
https://www.bib.irb.hr/1209753
https://www.bib.irb.hr/1209753
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1984 Aug . 81(16), 5204-5208.
Externí odkaz:
https://www.jstor.org/stable/24217
Publikováno v:
Indian Journal of Pediatrics. 88:611-611
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5024e9ca8cafe856140333fa98777a91
https://doi.org/10.1007/s12098-021-03706-8
https://doi.org/10.1007/s12098-021-03706-8
Publikováno v:
American Journal of Clinical Pathology. 150:S73-S74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30756e730b85446e9286f7e218f795b5
https://doi.org/10.1093/ajcp/aqy093.179
https://doi.org/10.1093/ajcp/aqy093.179
Autor:
Hataichanok Srivorakun, Nattaya Sae-ung, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Supan Fucharoen, Attawut Chaibunruang
Publikováno v:
Blood Cells, Molecules, and Diseases. 44:140-145
Hemoglobin (Hb) Lepore is a variant consisting of two alpha-globin and two deltabeta-globin chains. In heterozygote, it is associated with clinical findings of thalassemia minor but interactions with other hemoglobinopathies can lead to various clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85ce9d7138ad73c81f97a602f84735f8
https://doi.org/10.1016/j.bcmd.2009.11.008
https://doi.org/10.1016/j.bcmd.2009.11.008
Publikováno v:
Laboratory Medicine. 44:245-247
Hemoglobin (Hb) Lepore is a β+-thalassemic hemoglobin variant composed of 2 α-globin and 2 δβ-globin hybrid chains. Three common Hb Lepore variants have been identified based on the primary sequence of the fusion proteins. In most cases, diagnosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48e9911c8f2c5d648248415ae4d10d7a
https://doi.org/10.1309/lmfextw53plxib2u
https://doi.org/10.1309/lmfextw53plxib2u
Publikováno v:
Annals of hematology. 90(11)
We report the molecular basis and hematological phenotype associated with a hitherto undescribed interaction of hemoglobin (Hb) Lepore-Hollandia, Hb E and a deletion of three α-globin genes found in a 3-year-old Thai girl. She had mild anemia with H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d25511d929f9c0bd34e9021747f94a
https://pubmed.ncbi.nlm.nih.gov/21302111
https://pubmed.ncbi.nlm.nih.gov/21302111
Autor:
Piero Pucci, Antonio Malorni, G. Di Maro, Pasquale Esposito, Ernesto Grimaldi, P. Ferranti, Gennaro Marino, A Parlapiano, F. Scopacasa, M. De Caterina
Publikováno v:
Scopus-Elsevier
We describe an analytical protocol for characterizing the molecular structure of hemoglobin (Hb) Lepore variants by using two different mass-spectrometric approaches. The first method consists of direct examination of the chromatographically separate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7675629ad4454f41d62f9d1e69546d57
https://doi.org/10.1093/clinchem/38.8.1444
https://doi.org/10.1093/clinchem/38.8.1444